510(k) Report

FDA applicant

Medical Equipment Designs, Inc.

Mchenry, IL13 decisions1982–19910 recalls

FDA records 13 decisions for Medical Equipment Designs, Inc. (Mchenry, IL) from 1982 to 1991: 13 510(k) clearances. Most are in product codes BZG (Spirometer, Diagnostic) and HLH (Pupillometer, Manual). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ophthalmic panel, where it files most

How often FDA has decided Medical Equipment Designs, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Equipment Designs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medical Equipment Designs, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Medical Equipment Designs, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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